Canonical Allele Identifier: CA1142195853

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306112C= , CM000663.2:g.161306112C=	GRCh38
NC_000001.10:g.161275902C= , CM000663.1:g.161275902C=	GRCh37
NC_000001.9:g.159542526C=	NCBI36
NG_008055.1:g.8861G= , LRG_256:g.8861G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.560G=	ENSP00000488104.2:p.Arg187=
ENST00000533357.5:c.641G= MANE Select	ENSP00000432943.1:p.Arg214=
ENST00000672287.2:c.53G=	ENSP00000499818.2:p.Arg18=
ENST00000672602.2:c.641G=	ENSP00000500814.2:p.Arg214=
ENST00000674861.1:n.704G=
ENST00000463290.5:c.641G=	ENSP00000431538.1:p.Arg214=
ENST00000476410.1:n.101G=
ENST00000488271.1:n.79G=
ENST00000491222.5:c.53G=	ENSP00000431441.1:p.Arg18=
ENST00000526189.2:c.304G=
ENST00000533357.4:c.641G=	ENSP00000432943.1:p.Arg214=
NM_000530.6:c.641G= , LRG_256t1:c.641G=	NP_000521.2:p.Arg214=
NM_000530.7:c.641G=	NP_000521.2:p.Arg214=
NM_001315491.1:c.641G=	NP_001302420.1:p.Arg214=
XM_017001321.2:c.671G=	XP_016856810.1:p.Arg224=
NM_000530.8:c.641G= MANE Select	NP_000521.2:p.Arg214=
NM_001315491.2:c.641G=	NP_001302420.1:p.Arg214=